Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.150952481C>TCA004728KCNH2n.799G>A
n.394G>A
n.2334G>A
c.1501G>A (p.Asp501Asn)
c.481G>A (p.Asp161Asn)
c.1153G>A (p.Asp385Asn)
n.788G>A
n.806G>A
n.1724G>A
c.1201G>A (p.Asp401Asn)
c.1351G>A (p.Asp451Asn)
c.1324G>A (p.Asp442Asn)
ClinVar dbSNP
7g.150952481C>GCA004734KCNH2n.799G>C
n.394G>C
n.2334G>C
c.1501G>C (p.Asp501His)
c.481G>C (p.Asp161His)
c.1153G>C (p.Asp385His)
n.788G>C
n.806G>C
n.1724G>C
c.1201G>C (p.Asp401His)
c.1351G>C (p.Asp451His)
c.1324G>C (p.Asp442His)
ClinVar dbSNP

Number of alleles fetched